Annick Rossi

2.0k citations
11 papers · 847 · h-index 11

Impact in

    • Head and Neck Cancer Studies
  • Genetics top 5%
    • Chronic Lymphocytic Leukemia Research
    • Genomic variations and chromosomal abnormalities
    • BRCA gene mutations in cancer

Papers in

Annick Rossi

11 papers receiving 817 citations

Peers

Annick Rossi
Comparison fields: 5 of 53
  • Otorhinolaryngology 225
  • Genetics 174
  • Pathology and Forensic Medicine 237
  • Oncology 216
  • Neurology 47
Replace Csilla Neuchrist with:
Csilla Neuchrist Austria
Marianne Lodahl Denmark
Patricia Thompson United States
Steven C. Gerken United States
Cassin Kimmel Williams United States
Milhan Telatar United States
Martyna Adamowicz United Kingdom
Daniel Rosebrock United States
Greg B. Peters Australia
Zhongbo Yang United States
Annick Rossi relative to Csilla Neuchrist Austria Csilla Neuchrist's profile →
Citations per field
00.5×7.0×
Csilla Neuchrist · 1×
Citations per year

Countries citing papers authored by Annick Rossi

Since Specialization
Citations

This map shows the geographic impact of Annick Rossi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Annick Rossi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annick Rossi more than expected).

Fields of papers citing papers by Annick Rossi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Annick Rossi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Annick Rossi. The network helps show where Annick Rossi may publish in the future.

Co-authors

The 25 scholars most cited alongside Annick Rossi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Annick Rossi Line = papers co-authored together Annick Rossi links everyone, so they are left out of the graph.

All Works

11 of 11 papers shown
#Work
1 1988235
2 1994218
3 2002116
4 200483
5 200882
6 200433
7 200628
8 200217
9 200513
10 199412
11 200210

About Annick Rossi

Annick Rossi is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Genetics, Oncology and Surgery, having authored 11 papers that have together received 847 indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Sarcoma Diagnosis and Treatment (2 papers), Congenital heart defects research (2 papers), Viral-associated cancers and disorders (2 papers), Genomics and Rare Diseases (1 paper), Head and Neck Cancer Studies (1 paper) and Lung Cancer Research Studies (1 paper). The work is most often cited by research in Otorhinolaryngology (225 citations), Genetics (174 citations), Pathology and Forensic Medicine (237 citations), Oncology (216 citations) and Neurology (47 citations). Annick Rossi has collaborated with scholars based in France, Italy and Belgium. Frequent co-authors include C. Bigorgne, Bernard Lenormand, A Kunlin, M. Monconduit, Christian Bastard, Aspasia Stamatoullas, Hervé Tilly, Luca Morandi, Roberto Molinari and Patrizia Boracchi. Their work appears in journals such as European Journal of Human Genetics, Blood, Oncogene, Prenatal Diagnosis and Human Mutation.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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